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	<title>Pulmonary Fibrosis News Forums | Jan Riche | Activity</title>
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				<title>Jan Riche replied to the discussion Manufacturing Complex Organs Using a 3-D Printer in the forum Lung Transplantation</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/manufacturing-complex-organs-using-a-3-d-printer/#post-19724</link>
				<pubDate>Fri, 07 Jun 2019 18:44:47 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/manufacturing-complex-organs-using-a-3-d-printer/#post-19724"><span class="bb-reply-lable">Reply to</span> Manufacturing Complex Organs Using a 3-D Printer</a></p> <div class="bb-content-inr-wrap"><p>I would definitely take one, my Mom had a foreign object in her body for years, a pacemaker, not quite the same but close.  As for biodegradable, my whole body is biodegrade. If they could manufacture them maybe they wouldn&#8217;t have more likely to have said yes to my application. Besides, I am an unbearable optimist.<br />
Jan</p>
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				<title>Jan Riche replied to the discussion Recent diagnosis; so many questions in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/recent-diagnosis-so-many-questions/#post-19708</link>
				<pubDate>Fri, 07 Jun 2019 16:27:23 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/recent-diagnosis-so-many-questions/#post-19708"><span class="bb-reply-lable">Reply to</span> Recent diagnosis; so many questions</a></p> <div class="bb-content-inr-wrap"><p>Just went online and found a number for Imogene rentals. 1-855-213-4372. I would send a link to the web site but that is beyond my tech abilities. At first getting to understand the O2 process is confusing but it clears up eventually. At least that has been my experience.<br />
Jan</p>
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				<title>Jan Riche replied to the discussion Recent diagnosis; so many questions in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/recent-diagnosis-so-many-questions/#post-19704</link>
				<pubDate>Fri, 07 Jun 2019 16:04:41 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/recent-diagnosis-so-many-questions/#post-19704"><span class="bb-reply-lable">Reply to</span> Recent diagnosis; so many questions</a></p> <div class="bb-content-inr-wrap"><p>I too used Imogene. They are Medicare approved. They provided an in-home concentrator that went to 10 liters and a POC that went to 6 liters. What I really appreciated was the size of the in-home concentrator. It was small enough to fit in an over-head sized luggage so I did not have to worry about getting a unit at my destination. The POC had a&hellip;<span class="activity-read-more" id="activity-read-more-12888"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/recent-diagnosis-so-many-questions/#post-19704" rel="nofollow"> Read more</a></span></p>
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				<title>Jan Riche replied to the discussion Way to handle side effect nausea in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/way-to-handle-side-effect-nausea/#post-19703</link>
				<pubDate>Fri, 07 Jun 2019 15:30:43 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/way-to-handle-side-effect-nausea/#post-19703"><span class="bb-reply-lable">Reply to</span> Way to handle side effect nausea</a></p> <div class="bb-content-inr-wrap"><p>Meral ( @meraltemel ), I too had such serious side effects that I decided that my quality of life was more important than slowing down the progression of the disease. I stopped taking it. My doctor changed me to Esbriet. I don&#8217;t have any side effects from this medication. It is supposed to do the same thing.</p>
<p>I hope that is a possibility for&hellip;<span class="activity-read-more" id="activity-read-more-12887"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/way-to-handle-side-effect-nausea/#post-19703" rel="nofollow"> Read more</a></span></p>
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				<title>Jan Riche replied to the discussion can someone talk about the end days in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/can-someone-talk-about-the-end-days/#post-19627</link>
				<pubDate>Tue, 04 Jun 2019 23:28:26 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/can-someone-talk-about-the-end-days/#post-19627"><span class="bb-reply-lable">Reply to</span> can someone talk about the end days</a></p> <div class="bb-content-inr-wrap"><p>Lorena,<br />
Thank you for your reply. It comforts me to know I will not be gasping for breath at the end.   Breatlesssness (Lot of s&#8217;s there) is the thing I fear the most. If I can avoid it in any way I will do whatever I need to do. It takes me forever to do some things. I move at a snail&#8217;s pace. I used to do 10 minute showers now it&#8217;s an&hellip;<span class="activity-read-more" id="activity-read-more-12795"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/can-someone-talk-about-the-end-days/#post-19627" rel="nofollow"> Read more</a></span></p>
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				<title>Jan Riche posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/12774/#acomment-12777</link>
				<pubDate>Tue, 04 Jun 2019 17:46:44 -0500</pubDate>

									<content:encoded><![CDATA[<p>Hi Denny,<br />
I live in Tucson Arizona, my Galapagos trial is at Banner Hospital and the U of A. The Cleveland thing sounds interesting. How do you get in touch with them?</p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/deliassen/" data-bb-hp-profile="2892" rel="nofollow">Denny</a> posted an update <a class='bp-suggestions-mention' href='https://pulmonaryfibrosisnews.com/forums/members/janriche/' rel="nofollow">@janriche</a> I don&#8217;t know where you leave but they are looking for volunteers at the Cleveland Clinic now for BG00011, and I am soon doing the Galapagos study at University of Michigan GLPG 1690					]]></content:encoded>
				
				
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				<title>Jan Riche replied to the discussion Indalo Therapeutics Phase 1 Trial On IDL-2965 in the forum Flash Briefings &#38; Podcasts</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/indalo-therapeutics-phase-1-trial-on-idl-2965/#post-19622</link>
				<pubDate>Tue, 04 Jun 2019 17:25:37 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/indalo-therapeutics-phase-1-trial-on-idl-2965/#post-19622"><span class="bb-reply-lable">Reply to</span> Indalo Therapeutics Phase 1 Trial On IDL-2965</a></p> <div class="bb-content-inr-wrap"><p>I forgot to add that I conquered the flash briefings. Listened to my first today. </p>
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				<title>Jan Riche replied to the discussion Indalo Therapeutics Phase 1 Trial On IDL-2965 in the forum Flash Briefings &#38; Podcasts</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/indalo-therapeutics-phase-1-trial-on-idl-2965/#post-19620</link>
				<pubDate>Tue, 04 Jun 2019 17:10:33 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/indalo-therapeutics-phase-1-trial-on-idl-2965/#post-19620"><span class="bb-reply-lable">Reply to</span> Indalo Therapeutics Phase 1 Trial On IDL-2965</a></p> <div class="bb-content-inr-wrap"><p>Hi Charlene,<br />
I too hope the medical developments are in time to help you. I have grown fond of you through this forum. I appreciate your honesty and openness. Those are truly wonderful traits. </p>
<p>As for your question about clinical trials, I am hoping to qualify for a clinical trial called Galapagos. I am hoping that the name which reminds me&hellip;<span class="activity-read-more" id="activity-read-more-12772"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/indalo-therapeutics-phase-1-trial-on-idl-2965/#post-19620" rel="nofollow"> Read more</a></span></p>
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				<title>Jan Riche replied to the discussion Flash Briefing: IPF Patients Switching to Esbriet to Ofev Stopping Treatments, Possibly Due to Low BMI in the forum Flash Briefings &#38; Podcasts</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/flash-briefing-ipf-patients-switching-to-esbriet-to-ofev-stopping-treatments-possibly-due-to-low-bmi/#post-19541</link>
				<pubDate>Fri, 31 May 2019 15:30:56 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/flash-briefing-ipf-patients-switching-to-esbriet-to-ofev-stopping-treatments-possibly-due-to-low-bmi/#post-19541"><span class="bb-reply-lable">Reply to</span> Flash Briefing: IPF Patients Switching to Esbriet to Ofev Stopping Treatments, Possibly Due to Low BMI</a></p> <div class="bb-content-inr-wrap"><p>Hi Charlene,<br />
Interesting topic. I had to change from Ofev to Esbriet about a year ago.  The diarrhea got so bad it was unendurable. What quality of life I had was totally gone. I couldn&#8217;t leave home and couldn&#8217;t maintain my hygiene without difficulty. That was the determining factor. That experience left me apprehensive about Esbriet, fearful&hellip;<span class="activity-read-more" id="activity-read-more-12680"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/flash-briefing-ipf-patients-switching-to-esbriet-to-ofev-stopping-treatments-possibly-due-to-low-bmi/#post-19541" rel="nofollow"> Read more</a></span></p>
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				<title>Jan Riche replied to the discussion can someone talk about the end days in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/can-someone-talk-about-the-end-days/#post-19467</link>
				<pubDate>Wed, 29 May 2019 01:20:06 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/can-someone-talk-about-the-end-days/#post-19467"><span class="bb-reply-lable">Reply to</span> can someone talk about the end days</a></p> <div class="bb-content-inr-wrap"><p>I am not sure if I am on the right track but I believe I am in the end times. I did not get approved for a lung transplant so there is no option for me. My need for oxygen is going up quickly. Just being still requires 8/9 liters, if I need to get up I have to use a separate source of O2 at 6 liters which puts me at 14 liters. Just to sit up&hellip;<span class="activity-read-more" id="activity-read-more-12567"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/can-someone-talk-about-the-end-days/#post-19467" rel="nofollow"> Read more</a></span></p>
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				<title>Jan Riche replied to the discussion Healthy Solid Food Recipes in the forum Healthy Recipe Sharing</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/healthy-solid-food-recipes/#post-19183</link>
				<pubDate>Fri, 17 May 2019 16:48:19 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/healthy-solid-food-recipes/#post-19183"><span class="bb-reply-lable">Reply to</span> Healthy Solid Food Recipes</a></p> <div class="bb-content-inr-wrap"><p>Hi,<br />
Four years ago I was diagnosed as prediabetic. My doctor suggested a class that is a cooperative effort between the YMCA and the CDC (Center For Disease Control). They put me on a diet that simply had me restricting fat grams. There was an app that helped me count them. I found that my eating very naturally included healthy food, as the&hellip;<span class="activity-read-more" id="activity-read-more-12231"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/healthy-solid-food-recipes/#post-19183" rel="nofollow"> Read more</a></span></p>
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				<title>Jan Riche replied to the discussion A condition with no clear diagnostic criteria - Idiopathic in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/a-condition-with-no-clear-diagnostic-criteria-idiopathic/#post-19127</link>
				<pubDate>Tue, 14 May 2019 16:05:39 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/a-condition-with-no-clear-diagnostic-criteria-idiopathic/#post-19127"><span class="bb-reply-lable">Reply to</span> A condition with no clear diagnostic criteria - Idiopathic</a></p> <div class="bb-content-inr-wrap"><p>Hi Army Pete,<br />
Love the Army, was a WAC in the Vietnam era, but did not serve in Vietnam Nam or Japan where a lot of support served. I believe the Army made me grow up. Certainly gave me an education through the GI bill </p>
<p>As to OFEV, I had the same problem but changed to Esbriet and no side effects. No way to know if it&#8217;s slowing down the IPF&hellip;<span class="activity-read-more" id="activity-read-more-12163"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/a-condition-with-no-clear-diagnostic-criteria-idiopathic/#post-19127" rel="nofollow"> Read more</a></span></p>
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				<title>Jan Riche replied to the discussion &#34;Surviving IPF&#34; is More Than Just the Physical Impact of the Disease in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/surviving-ipf-just-physical-impact-disease/#post-19076</link>
				<pubDate>Sat, 11 May 2019 15:32:42 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/surviving-ipf-just-physical-impact-disease/#post-19076"><span class="bb-reply-lable">Reply to</span> "Surviving IPF" is More Than Just the Physical Impact of the Disease</a></p> <div class="bb-content-inr-wrap"><p>Charlene,<br />
I am truly sorry to hear that it&#8217;s still stressful for you. It must be difficult to see her on a regular basis. My heart goes out to you and I hope additional time will soften the blow.<br />
Jan R</p>
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				<title>Jan Riche replied to the discussion &#34;Surviving IPF&#34; is More Than Just the Physical Impact of the Disease in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/surviving-ipf-just-physical-impact-disease/#post-19065</link>
				<pubDate>Fri, 10 May 2019 14:59:10 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/surviving-ipf-just-physical-impact-disease/#post-19065"><span class="bb-reply-lable">Reply to</span> "Surviving IPF" is More Than Just the Physical Impact of the Disease</a></p> <div class="bb-content-inr-wrap"><p>Hi Charlene, I know how it feels to be  deeply hurt by someone close. In my 77 years it has happened. Sometimes my relationship has survived and at other times not so much. For me,it would be important to know if the person was just frustrated or meant to hurt me. I don&#8217;t know exactly how I would know and I don&#8217;t know if I have assessed it&hellip;<span class="activity-read-more" id="activity-read-more-12095"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/surviving-ipf-just-physical-impact-disease/#post-19065" rel="nofollow"> Read more</a></span></p>
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				<title>Jan Riche replied to the discussion Portable oxygen in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/portable-oxygen/#post-19027</link>
				<pubDate>Thu, 09 May 2019 15:59:55 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/portable-oxygen/page/2/#post-19027"><span class="bb-reply-lable">Reply to</span> Portable oxygen</a></p> <div class="bb-content-inr-wrap"><p>Hi,</p>
<p>This is my second attempt to use this forum. Hope it works. Oxygen suppliers have been one of the most trying thing about my IPF. Luckily I have had really good advocates that worked for my pulmonologists. One from Jewish National in Denver worked to get me set up with Enogen to rent a home concentrator and POC. I started out with&hellip;<span class="activity-read-more" id="activity-read-more-12065"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/portable-oxygen/#post-19027" rel="nofollow"> Read more</a></span></p>
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				<title>Jan Riche replied to the discussion Tips for Making A Shower Easier with Pulmonary Fibrosis. in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/tips-for-making-a-shower-easier-with-pulmonary-fibrosis/#post-18521</link>
				<pubDate>Tue, 16 Apr 2019 16:35:47 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/tips-for-making-a-shower-easier-with-pulmonary-fibrosis/#post-18521"><span class="bb-reply-lable">Reply to</span> Tips for Making A Shower Easier with Pulmonary Fibrosis.</a></p> <div class="bb-content-inr-wrap"><p>Hi Charlene,</p>
<p>My IPF has accelerated over the past six months, my O2 has gone from 6 liters to 7-9 depending on activity. Even at 9 I have to go slowly with rests to let my sats recover. Showering has become an issue. I&#8217;m in a wheelchair because walking drops my O2 sats to low 70&#8217;s almost immediately.</p>
<p>To shower I get everything set up,&hellip;<span class="activity-read-more" id="activity-read-more-11369"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/tips-for-making-a-shower-easier-with-pulmonary-fibrosis/#post-18521" rel="nofollow"> Read more</a></span></p>
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				<title>Jan Riche replied to the discussion Dying from IPF in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/dying-from-ipf/#post-18360</link>
				<pubDate>Sat, 13 Apr 2019 01:41:48 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/dying-from-ipf/page/2/#post-18360"><span class="bb-reply-lable">Reply to</span> Dying from IPF</a></p> <div class="bb-content-inr-wrap"><p>Hi Bill,</p>
<p>I was sorry to hear about your struggles, makes my journey sound like a walk in the park. I am 76 (77 next month) and my O2 requirement has just gone to 7-9 liters depending, so I don&#8217;t do much that requires moving, which means that I don&#8217;t cook any more. I miss that a lot but didn&#8217;t have to sell my pots and pans.</p>
<p>Luckily I love&hellip;<span class="activity-read-more" id="activity-read-more-11154"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/dying-from-ipf/#post-18360" rel="nofollow"> Read more</a></span></p>
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				<title>Jan Riche replied to the discussion Hearing Others&#039; IPF Story: Pros &#38; Cons. in the forum Caregivers and Spouses</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/hearing-others-ipf-story-pros-cons/#post-18267</link>
				<pubDate>Wed, 10 Apr 2019 00:06:17 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/hearing-others-ipf-story-pros-cons/#post-18267"><span class="bb-reply-lable">Reply to</span> Hearing Others' IPF Story: Pros & Cons.</a></p> <div class="bb-content-inr-wrap"><p>Hi Charlene, I&#8217;m sorry you had this experience, I know how much I need to forget for awhile that I have this condition. But I also know how difficult I find it to be in the company of a negative attitude, I don&#8217;t seem to care so much about the content of the conversation as I do the attitude.  My friends and I can talk about this disease and&hellip;<span class="activity-read-more" id="activity-read-more-11042"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/hearing-others-ipf-story-pros-cons/#post-18267" rel="nofollow"> Read more</a></span></p>
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				<title>Jan Riche replied to the discussion Achalasia and Lung Transplantation in the forum Lung Transplantation</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/18246/#post-18266</link>
				<pubDate>Tue, 09 Apr 2019 23:32:11 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/18246/#post-18266"><span class="bb-reply-lable">Reply to</span> Achalasia and Lung Transplantation</a></p> <div class="bb-content-inr-wrap"><p>Hi Mark,</p>
<p>My esophageal motility disorder is a slow peristalsis, my esophagus is slow but not blocked.  The major thing I notice is how long it takes to eat.  The worst part of eating is that my food never tastes right, I think that is due to my meds. I keep thinking with a reduced intake I should lose weight but my lack of exercise seems to&hellip;<span class="activity-read-more" id="activity-read-more-11041"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/18246/#post-18266" rel="nofollow"> Read more</a></span></p>
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				<title>Jan Riche replied to the discussion Achalasia and Lung Transplantation in the forum Lung Transplantation</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/18246/#post-18263</link>
				<pubDate>Tue, 09 Apr 2019 17:32:25 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/18246/#post-18263"><span class="bb-reply-lable">Reply to</span> Achalasia and Lung Transplantation</a></p> <div class="bb-content-inr-wrap"><p>I was diagnosed with esophageal motility disorder last year and was eliminated as a candidate for lung transplant. My age may have been a contributing factor. I was 76 years old.  Everything else was good, no other physical problems.</p>
<p>I was depressed for 10 days after they told me, but I have decided that everyone dies from something and this&hellip;<span class="activity-read-more" id="activity-read-more-11037"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/18246/#post-18263" rel="nofollow"> Read more</a></span></p>
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				<title>Jan Riche became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/10041/</link>
				<pubDate>Sat, 09 Mar 2019 17:22:35 -0600</pubDate>

				
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